Acetyl chloride → HCID 18368130, compound

HRID 379833Notes

Reaction equation

HRID 379833 reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:12](=[O:23])[C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([O:21][CH3:22])=[O:20])[CH:14]=1.[C:24](Cl)(=[O:26])[CH3:25]>C(OCC)(=O)C>[C:24]([NH:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:12](=[O:23])[C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([O:21][CH3:22])=[O:20])[CH:14]=1)(=[O:26])[CH3:25]

Participants

4

Reactant 2

HCID 6367Acetyl chlorideHCID 18368014HCID 18368014, compound

Product 1

HCID 18368130HCID 18368130, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

The title compound was prepared according to the procedure described in Example 19 employing 3-amino-6-chloro-2-(3-methoxycarbonylbenzoyl)indole (Example 133) and acetyl chloride. m.p.: 190-193° C. (ethyl acetate)

Sources & evidence

ORD record
ord-d86bdfb5cdcc47aaa6b025724feeeec9
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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